Instem - Information Solutions For Life

Solutions

• Provantis
• Submit SEND solution
• Toxicology Resource Planning
• Information Management
• Regulatory

Overview
Instem's Clinical Pathology solution is based on the Provantis™ Clinical Pathology product. This product provides bench-level functionality for the collection and processing of Clinical Pathology data, as well as further ‘Supervisor’ review, amend and release options to ensure quality results are released back to the study.

Quality Control material can be defined, maintained and used throughout the system to check instrument performance prior to and / or during animal data collection.

The system is driven by the protocol entered in the General Toxicology product, directing sample collection in the animal room and subsequent analysis within the Clinical Pathology laboratory. This level of product integration ensures there is no need to re-enter protocol details. Ad-hoc study samples may also be run as required.

Clinical Pathology specific reports are held within the ‘Supervisor’ module and provide;

• Analytical ‘run’ reports to mimic instrument data print-outs
• Study based animal result and sample raw data reports
• QC based raw data and historical analysis reports

Final study reports are provided from the Provantis™ Tables & Statistics module and integrate Clinical Pathology data with all other study data

Key features

• Configurable instrument interfacing software (uni and bi-directional)
• Clear spreadsheet style layout of result data
• Real time display of instrument data capture
• QC collection, validation and export
• Different display modes (results / exceptions) for efficient data review
• Measurement tagging for easy addition of comments and results
• Security controlled data changes
• Full audit trailing
  

Latest features

• Production of sample labels (including bar-codes) through Provantis™ Labeling Module
• Electronic signature on review sign-off steps
• Screen lock-out facilities throughout system
• Security enhancements in data transfers
• QC lot maintenance, QC data storage and QC reports
• Randomised / Counter-balanced collection lists
• Dilution factor / audit trailing utility
• Optional additional levels of data review